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A Gold Interdigitated Microelectrodes Fabricated on Polyhydroxybutyrate Substrate for the Determination of Urea Using Impedimetric Measurements

机译:用阻抗测定法在聚羟基丁酸酯基质上制备的金指状微电极用于尿素的测定

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摘要

A novel impedimetric biosensor was microfabricated for the selective and quantitative determination of urea by immobilizing urease onto the 1 cm$,times ,$2 cm$, times ,$0.5 mm PHB substrate which was patterned with gold interdigitated electrode arrays (IDAs) using a combination of photolithography, etching, and thermal evaporation processes. In this study, urease was covalently immobilized onto the gold IDAs functionalized with 10-carboxyl-1-decanethiol (CDT) and similarly, onto gold IDAs functionalized with CDT-polypropylenimine dotriacontaamine dendrimer (Generation 4.0, DAB-Am-32) for monitoring factors that affect urease immobilization. The response studies were carried out as a function of urea concentration with impedimetric measurements. These two immobilization techniques were introduced to assay for in vitro urea and evaluate the two immobilization technique in terms of their repeatability, linear dynamic range, temperature and pH stability. The CDT-urease biosensor displayed linearity for assayed urea up to 10 mM with a response time (${rm t} _{95}$) of 2 s and yielded a ${rm K} _{{rm m}({rm app})}$ of 0.7 mM, indicating the urease enzyme immobilized using CDT onto the PHB IDA surface had a high affinity to urea. The CDT-DAB-Urease biosensor exhibited a dynamic linear range of 0.10 – 300.0 mM, which represented a 30-fold increase in linear dynamic urea range compared to the biosensor with the CDT-urease. The CDT-DAB-Urease yielded a ${rm K} _{{rm m}({rm app})}$ of 2.2 mM, which is not significantly different from that for the native, solution-borne enzyme (3 mM), thereby indicating an affinity to urea. Prelimin-nry results suggest that the coupling of the CDT-DAB immobilization technique with microfabrication technology can offer large scale production of PHB urea biosensor.
机译:通过将尿素酶固定在1厘米2倍,2厘米2倍,0.5毫米的PHB基板上,微细地制造了一种新型的阻抗生物传感器,用于尿素的选择性和定量测定,PHB基板上用金叉指电极阵列(IDA)组合使用光刻,蚀刻和热蒸发工艺。在这项研究中,尿素酶被共价固定在用10-羧基-1-癸硫醇(CDT)功能化的金IDA上,同样地,固定在用CDT-聚丙烯酰胺亚胺酸三叉胺树状大分子(Generation 4.0,DAB-Am-32)官能化的金IDA上。影响尿素酶固定化。根据尿素浓度和阻抗测量结果进行反应研究。将这两种固定化技术引入体外尿素分析中,并从其重复性,线性动态范围,温度和pH稳定性方面评估了两种固定化技术。 CDT-脲酶生物传感器对尿素浓度高达10 mM的线性显示时间为2秒,响应时间($ {rm t} _ {95} $)为$ {rm K} _ {{rm m}({rm app}}} $为0.7 mM,表明使用CDT固定在PHB IDA表面上的脲酶对尿素的亲和力高。 CDT-DAB-脲酶生物传感器的动态线性范围为0.10-300.0 mM,与带有CDT脲酶的生物传感器相比,线性动态尿素范围增加了30倍。 CDT-DAB-尿素酶产生的$ {rm K} _ {{rm m}({rm app})} $为2.2 mM,与天然的溶液传播酶(3 mM)并无显着差异。 ,从而表明对尿素有亲和力。初步结果表明,CDT-DAB固定化技术与微细加工技术的结合可以提供PHB尿素生物传感器的大规模生产。

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